Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Related Concept Videos

Three-Dimensional Microscopy in Microbiology01:28

Three-Dimensional Microscopy in Microbiology

Three-dimensional imaging techniques are essential in cell biology, allowing researchers to visualize intricate cellular structures with high resolution. Two prominent methods, Differential Interference Contrast Microscopy (DIC) and Confocal Scanning Laser Microscopy (CSLM), provide distinct advantages for imaging live and thick specimens, respectively.Differential Interference Contrast MicroscopyDIC microscopy enhances contrast in transparent, unstained samples by converting phase...
Super-resolution Fluorescence Microscopy01:37

Super-resolution Fluorescence Microscopy

Super-resolution fluorescence microscopy (SRFM) provides a better resolution than conventional fluorescence microscopy by reducing the point spread function (PSF). PSF is the light intensity distribution from a point that causes it to appear blurred. Due to PSF, each fluorescing point appears bigger than its actual size, and it is the PSF interference of nearby fluorophores that causes the blurred image. Various approaches to achieving higher resolution through SRFM have recently been developed.
Two-Dimensional Microscopy in Microbiology01:29

Two-Dimensional Microscopy in Microbiology

Two-dimensional (2D) microscopy encompasses a range of optical techniques that capture images within a single focal plane, offering detailed representations of microscopic structures. These techniques are essential in biological and medical research, enabling the visualization of cellular and subcellular structures with different levels of contrast and specificity.There are several major types of 2D microscopy, each with strengths and applications.Bright-Field MicroscopyBright-field microscopy...
Immunofluorescence Microscopy01:12

Immunofluorescence Microscopy

A fluorescence microscope uses fluorescent chromophores called fluorochromes, which can absorb energy from a light source and then emit this energy as visible light. Fluorochromes include naturally fluorescent substances (such as chlorophylls) and fluorescent stains that are added to the specimen to create contrast. Dyes such as Texas red and FITC are examples of fluorochromes. Other examples include the nucleic acid dyes 4’,6’-diamidino-2-phenylindole (DAPI), and acridine orange.
The...
Confocal Fluorescence Microscopy01:16

Confocal Fluorescence Microscopy

Confocal microscopy is an advanced microscopic technique. The prime advantage of the confocal microscope over other microscopy techniques is its ability to block the out-of-focus light from the illuminated samples using pinholes. It is widely used with fluorescence optics to obtain high-resolution, sharp contrast images. Unlike optical microscopes, confocal microscopes use a focused beam of light laser to scan the entire sample surface at different z-planes. These microscopes are, therefore,...

You might also read

Related Articles

Articles linked to this work by shared authors, journal, and citation graph.

Sort by
Same author

From repair to relay: Human retinal organoids re-couple a severed optic nerve.

Cell stem cell·2026
Same author

Micromechanical characterisation of osteoarthritic subchondral bone by micropillar compression.

Acta biomaterialia·2026
Same author

Soldier Beetle Larvae Are Much More Common in the Fossil Record than Previously Anticipated.

Insects·2026
Same author

A True Bug with a True but Unique Chela in 100 Million-Year-Old Amber.

Insects·2026
Same author

Polychaete annelids from the earliest Cambrian Period.

Proceedings of the National Academy of Sciences of the United States of America·2026
Same author

Reconstructing tumor tissues in 3D: From organoids to bioengineered niches.

Cell stem cell·2026

Related Experiment Video

Updated: May 29, 2026

An Analytical Tool that Quantifies Cellular Morphology Changes from Three-dimensional Fluorescence Images
10:00

An Analytical Tool that Quantifies Cellular Morphology Changes from Three-dimensional Fluorescence Images

Published on: August 31, 2012

Autofluorescence imaging, an excellent tool for comparative morphology.

Joachim T Haug1, Carolin Haug, Verena Kutschera

  • 1Biosystematic Documentation, University of Ulm, Ulm, Germany. joachim.haug@yale.edu

Journal of Microscopy
|September 3, 2011
PubMed
Summary

Autofluorescence imaging offers a fast, high-resolution method for documenting arthropod and fossil morphology. This technique enhances contrast and detail without specimen preparation, providing valuable data for taxonomic studies.

More Related Videos

Light Sheet-based Fluorescence Microscopy of Living or Fixed and Stained Tribolium castaneum Embryos
10:15

Light Sheet-based Fluorescence Microscopy of Living or Fixed and Stained Tribolium castaneum Embryos

Published on: April 28, 2017

Visualization of Motor Axon Navigation and Quantification of Axon Arborization In Mouse Embryos Using Light Sheet Fluorescence Microscopy
08:56

Visualization of Motor Axon Navigation and Quantification of Axon Arborization In Mouse Embryos Using Light Sheet Fluorescence Microscopy

Published on: May 11, 2018

Related Experiment Videos

Last Updated: May 29, 2026

An Analytical Tool that Quantifies Cellular Morphology Changes from Three-dimensional Fluorescence Images
10:00

An Analytical Tool that Quantifies Cellular Morphology Changes from Three-dimensional Fluorescence Images

Published on: August 31, 2012

Light Sheet-based Fluorescence Microscopy of Living or Fixed and Stained Tribolium castaneum Embryos
10:15

Light Sheet-based Fluorescence Microscopy of Living or Fixed and Stained Tribolium castaneum Embryos

Published on: April 28, 2017

Visualization of Motor Axon Navigation and Quantification of Axon Arborization In Mouse Embryos Using Light Sheet Fluorescence Microscopy
08:56

Visualization of Motor Axon Navigation and Quantification of Axon Arborization In Mouse Embryos Using Light Sheet Fluorescence Microscopy

Published on: May 11, 2018

Area of Science:

  • Morphological studies
  • Imaging techniques
  • Biophotonics

Background:

  • Traditional methods for documenting morphology can be time-consuming and may require specimen preparation.
  • Autofluorescence imaging presents an alternative with potential for enhanced contrast and detail.

Purpose of the Study:

  • To present methods for documenting (exo-)morphology using autofluorescence imaging.
  • To evaluate autofluorescence imaging as a fast, high-resolution documentation tool for various taxa and fossils.

Main Methods:

  • Application of autofluorescence imaging with composite imaging for arthropods and other taxa.
  • Utilizing different wavelengths to enhance specific structures.
  • Adapting techniques for dried, embedded, or liquid-preserved specimens, and fossils.

Main Results:

  • Autofluorescence imaging provides homogenous illumination and better contrast compared to conventional photography.
  • The technique is applicable to diverse specimens, including rare and type specimens, without preparation.
  • Significant contrast enhancement was observed for fossils, revealing fine details.

Conclusions:

  • Autofluorescence imaging is a powerful, easy, and fast tool for morphological studies.
  • 'Life-colour' fluorescence offers additional information, reducing the need for complex methods.
  • The study explores and evaluates fluorescence macrophotography and microscopy techniques, suggesting future improvements.